000 | 02018 a2200649 4500 | ||
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005 | 20250517113747.0 | ||
264 | 0 | _c20171221 | |
008 | 201712s 0 0 eng d | ||
022 | _a1879-1484 | ||
024 | 7 |
_a10.1016/j.atherosclerosis.2016.08.037 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aGrenkowitz, Thomas | |
245 | 0 | 0 |
_aClinical characterization and mutation spectrum of German patients with familial hypercholesterolemia. _h[electronic resource] |
260 |
_bAtherosclerosis _c10 2016 |
||
300 |
_a88-93 p. _bdigital |
||
500 | _aPublication Type: Journal Article | ||
650 | 0 | 4 | _aAdult |
650 | 0 | 4 | _aAlleles |
650 | 0 | 4 |
_aApolipoproteins B _xgenetics |
650 | 0 | 4 |
_aCholesterol, LDL _xblood |
650 | 0 | 4 | _aDNA Mutational Analysis |
650 | 0 | 4 | _aExons |
650 | 0 | 4 | _aFemale |
650 | 0 | 4 | _aGenetic Association Studies |
650 | 0 | 4 | _aGenetic Variation |
650 | 0 | 4 | _aGermany |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 |
_aHyperlipoproteinemia Type II _xblood |
650 | 0 | 4 | _aMale |
650 | 0 | 4 | _aMiddle Aged |
650 | 0 | 4 | _aMutation |
650 | 0 | 4 | _aMutation, Missense |
650 | 0 | 4 | _aPhenotype |
650 | 0 | 4 |
_aProprotein Convertase 9 _xgenetics |
650 | 0 | 4 |
_aProprotein Convertases _xgenetics |
650 | 0 | 4 | _aROC Curve |
650 | 0 | 4 |
_aReceptors, LDL _xgenetics |
650 | 0 | 4 |
_aSerine Endopeptidases _xgenetics |
700 | 1 | _aKassner, Ursula | |
700 | 1 | _aWühle-Demuth, Marion | |
700 | 1 | _aSalewsky, Bastian | |
700 | 1 | _aRosada, Adrian | |
700 | 1 | _aZemojtel, Tomasz | |
700 | 1 | _aHopfenmüller, Werner | |
700 | 1 | _aIsermann, Berend | |
700 | 1 | _aBorucki, Katrin | |
700 | 1 | _aHeigl, Franz | |
700 | 1 | _aLaufs, Ulrich | |
700 | 1 | _aWagner, Stephan | |
700 | 1 | _aKleber, Marcus E | |
700 | 1 | _aBinner, Priska | |
700 | 1 | _aMärz, Winfried | |
700 | 1 | _aSteinhagen-Thiessen, Elisabeth | |
700 | 1 | _aDemuth, Ilja | |
773 | 0 |
_tAtherosclerosis _gvol. 253 _gp. 88-93 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1016/j.atherosclerosis.2016.08.037 _zAvailable from publisher's website |
999 |
_c26390882 _d26390882 |